{"title":"Synthesis of 99mTc-labeled polyaspartic acid/silica nanoassembly as a potential probe for bone imaging","authors":"Noha A. Bayoumi, Marwa E. Sayyed, Wael M. Darwish","doi":"10.1186/s13065-025-01508-z","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p>Due to the efficient bone targeting of mesoporous silica nanoparticles (MSNs) and polyaspartic acid (PASP), <sup>99m</sup>Tc- labeled polyaspartic acid coated mesoporous silica nanoparticles (PASP-mSiO<sub>2</sub>-DTPA-<sup>99m</sup>Tc) are proposed as a potential probe for bone imaging.</p><h3>Methods</h3><p>Polyaspartic acid-conjugated silica nanoparticles (PASP-mSiO<sub>2</sub>) were synthesized using aqueous carbodiimide chemistry and characterized by ATR-FTR, FE-SEM, EDX, TEM, TGA and XRD. Radiolabeling of the produced nanoassembly with <sup>99m</sup>Tc was carried out via a simple DTPA chelation procedure. Aqueous dispersion of the radiolabeled nanoparticles was intravenously injected into normal mice and the bone targeting efficiency was evaluated.</p><h3>Results</h3><p>The PASP-mSiO<sub>2</sub> nanoassembly was efficiently synthesized and radiolabeled with <sup>99m</sup>Tc with a high radiochemical yield (92 ± 0.5%) and sufficient in vitro stability in PBS and FBS for up to 24 h. In vivo biodistribution studies revealed a significant enhancement of radioactivity bone uptake after intravenous injection of PASP-mSiO<sub>2</sub>-DTPA-<sup>99m</sup>Tc compared to radiolabeled uncoated MSNs (mSiO<sub>2</sub>-DTPA-<sup>99m</sup>Tc), (13 ± 0.6% IA/gram and 5.4 ± 0.4, respectively).</p><h3>Conclusion</h3><p>PASP endowed MSNs with enhanced biocompatibility and highly selective bone targeting. Therefore, the proposed PASP-mSiO<sub>2</sub>-DTPA-<sup>99m</sup>Tc nanoassembly has immense potential in the field of bone- imaging via single photon emitting computed tomography (SPECT).</p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div><div><p>.</p></div></div></figure></div></div>","PeriodicalId":496,"journal":{"name":"BMC Chemistry","volume":"19 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bmcchem.biomedcentral.com/counter/pdf/10.1186/s13065-025-01508-z","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1186/s13065-025-01508-z","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose
Due to the efficient bone targeting of mesoporous silica nanoparticles (MSNs) and polyaspartic acid (PASP), 99mTc- labeled polyaspartic acid coated mesoporous silica nanoparticles (PASP-mSiO2-DTPA-99mTc) are proposed as a potential probe for bone imaging.
Methods
Polyaspartic acid-conjugated silica nanoparticles (PASP-mSiO2) were synthesized using aqueous carbodiimide chemistry and characterized by ATR-FTR, FE-SEM, EDX, TEM, TGA and XRD. Radiolabeling of the produced nanoassembly with 99mTc was carried out via a simple DTPA chelation procedure. Aqueous dispersion of the radiolabeled nanoparticles was intravenously injected into normal mice and the bone targeting efficiency was evaluated.
Results
The PASP-mSiO2 nanoassembly was efficiently synthesized and radiolabeled with 99mTc with a high radiochemical yield (92 ± 0.5%) and sufficient in vitro stability in PBS and FBS for up to 24 h. In vivo biodistribution studies revealed a significant enhancement of radioactivity bone uptake after intravenous injection of PASP-mSiO2-DTPA-99mTc compared to radiolabeled uncoated MSNs (mSiO2-DTPA-99mTc), (13 ± 0.6% IA/gram and 5.4 ± 0.4, respectively).
Conclusion
PASP endowed MSNs with enhanced biocompatibility and highly selective bone targeting. Therefore, the proposed PASP-mSiO2-DTPA-99mTc nanoassembly has immense potential in the field of bone- imaging via single photon emitting computed tomography (SPECT).
期刊介绍:
BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family.
Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.